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Crystalline forms of 1-chloro-4-(beta-D-glucopyranos-1-yl)-2-[4-ethynyl-benzyl)-benzene, methods for its preparation and the use thereof for preparing medicaments

Active Publication Date: 2007-03-08
BOEHRINGER INGELHEIM INT GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0013] In a first aspect the present invention relates to a crystalline complex between one or

Problems solved by technology

Another problem which may arise in the grinding process for preparing the desired pharmaceutical formulation is the input of energy caused by this process and the stress on the surface of the crystals.
This may in certain circumstances lead to polymorphous changes, to amorphization or to a change in the crystal lattice.
The absorption of moisture reduces the content of pharmaceutically active substance as a result of the increased weight caused by the uptake of water.

Method used

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  • Crystalline forms of 1-chloro-4-(beta-D-glucopyranos-1-yl)-2-[4-ethynyl-benzyl)-benzene, methods for its preparation and the use thereof for preparing medicaments
  • Crystalline forms of 1-chloro-4-(beta-D-glucopyranos-1-yl)-2-[4-ethynyl-benzyl)-benzene, methods for its preparation and the use thereof for preparing medicaments
  • Crystalline forms of 1-chloro-4-(beta-D-glucopyranos-1-yl)-2-[4-ethynyl-benzyl)-benzene, methods for its preparation and the use thereof for preparing medicaments

Examples

Experimental program
Comparison scheme
Effect test

example i

[0100]

(5-bromo-2-chloro-phenyl)-(4-methoxy-phenyl)-methanone

[0101] 38.3 mL oxalyl chloride and 0.8 mL dimethylformamide are added to a mixture of 100 g of 5-bromo-2-chloro-benzoic acid in 500 mL dichloromethane. The reaction mixture is stirred for 14 h, then filtered and separated from all volatile constituents in the rotary evaporator. The residue is dissolved in 150 mL dichloromethane, the solution is cooled to −5° C., and 46.5 g of anisole are added. Then 51.5 g of aluminum trichloride are added batchwise so that the temperature does not exceed 5° C. The solution is stirred for another 1 h at 1-5° C. and then poured onto ice. The organic phase is separated and the aqueous phase is extracted another three times with dichloromethane. The combined organic phases are washed with aqueous 1 M hydrochloric acid, twice with 1 M sodium hydroxide solution and with brine.

[0102] Then the organic phase is dried, the solvent is removed and the residue is recrystallised from ethanol.

[0103] Y...

example ii

[0105]

4-bromo-1-chloro-2-(4-methoxy-benzyl)-benzene

[0106] A solution of 86.2 g (5-bromo-2-chloro-phenyl)-(4-methoxy-phenyl)-methanone and 101.5 mL triethylsilane in 75 mL dichloromethane and 150 mL acetonitrile is cooled to 10° C. Then with stirring 50.8 mL of boron trifluoride etherate are added so that the temperature does not exceed 20° C. The solution is stirred for 14 h at ambient temperature, before another 9 mL triethylsilane and 4.4 mL boron trifluoride etherate are added. The solution is stirred for a further 3 h at 45-50° C. and then cooled to ambient temperature. A solution of 28 g potassium hydroxide in 70 mL water is added and the mixture is stirred for 2 h. Then the organic phase is separated and the aqueous phase is extracted three times with diisopropylether. The combined organic phases are washed twice with 2 M potassium hydroxide solution and once with brine and then dried over sodium sulfate. After the solvent has been eliminated the residue is stirred in ethanol...

example iii

[0109]

4-(5-bromo-2-chloro-benzyl)-phenol

[0110] A solution of 14.8 g 4-bromo-1-chloro-2-(4-methoxy-benzyl)-benzene in 150 mL dichloromethane is cooled in an ice bath. Then 50 mL of a 1 M solution of boron tribromide in dichloromethane are added, and the solution is stirred for 2 h at ambient temperature. The solution is then cooled in an ice bath again, and saturated potassium carbonate solution is added dropwise. At ambient temperature the mixture is adjusted with aqueous 1 M hydrochloric acid to a pH of 1, the organic phase is separated and the aqueous phase is extracted another three times with ethyl acetate. The combined organic phases are dried over sodium sulfate and the solvent is removed completely.

[0111] Yield: 13.9 g (98% of theory)

[0112] Mass spectrum (ESI−): m / z=295 / 297 / 299 (Br+Cl) [M−H]−

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Abstract

The invention relates to a crystalline hydrate of 1-chloro-4-(β-D-glucopyranos-1-yl)-2-(4-ethynyl-benzyl)-benzene and to crystalline complexes between 1-chloro-4-(β-D-glucopyranos-1-yl)-2-(4-ethynyl-benzyl)-benzene and a natural amino acid, to methods for the preparation thereof, as well as to uses thereof for preparing medicaments.

Description

[0001] This application claims priority benefit to EP 05019527, filed Sep. 8, 2005, which is incorporated herein in its entirety. [0002] The invention relates to a crystalline hydrate and to crystalline complexes of 1-chloro-4-(β-D-glucopyranos-1-yl)-2-(4-ethynyl-benzyl)-benzene, to methods for the preparation thereof, as well as to the use thereof for preparing medicaments. BACKGROUND OF THE INVENTION [0003] The compound 1-chloro-4-(β-D-glucopyranos-1-yl)-2-(4-ethynyl-benzyl)-benzene (in the following referred to it as “compound A”) is described in the international patent application WO 2005 / 092877 and has the chemical structure according to formula A [0004] The compounds described therein have a valuable inhibitory effect on the sodium-dependent glucose cotransporter SGLT, particularly SGLT2. The method of manufacture of the compound A as described therein does not yield a crystalline form. [0005] A certain pharmaceutical activity is of course the basic prerequisite to be fulfil...

Claims

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Application Information

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IPC IPC(8): A61K31/7034C07H5/04
CPCC07D309/10C07H7/00C07H5/04A61P3/04A61P3/06A61P3/08A61P7/10A61P9/04A61P9/06A61P9/10A61P9/12A61P3/10A61K31/351
Inventor ECKHARDT, MATTHIASHIMMELSBACH, FRANKBUTZ, TANJASCHUEHLE, MARTINMARTIN, HANS-JUERGEN
Owner BOEHRINGER INGELHEIM INT GMBH
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